Cancer.gov
 
Cancer.gov The CIRB logo Home How to Join Studies
Participant's Area FAQs Contacts
bar The CIRB Initiative Board Member Roster CIRB Feedback Form
bar bar How it Works Meeting Information Links
bar Activity Updates
  bar bar bar bar
      bar bar
Benefits to Participating Institutions
  • Participating institutions can develop their own procedure for conducting a facilitated review, as long as the procedure remains within the parameters of the Division of Responsibilities document.
  • The IRB chair alone or a subcommittee of the full Board can carry out the local review without convening the full Board.
  • IRB staff will not have to distribute multiple sets of documents, obtain primary reviewers' reviews from Local IRB Members (the documents will be on this website), negotiate changes with the investigator, or manage the consequences of deferring or tabling studies.
  • If the person(s) conducting the facilitated review concludes that there are no concerns about local context and accepts the CIRB review, the CIRB becomes the IRB of record for that study and will be responsible for reviewing subsequent amendments, continuing reviews and serious adverse events.

  • Should the local IRB wish to discuss a study in full convened session, it can still use the CIRB review materials as a resource.

bar   back to top back to top arrow   
About this site Privacy Policy Contact CIRB Webmaster bar bar bar
 
Cancer.gov National Institutes of Health Department of Health and Human Services FirstGov.gov